S. Lesage
Epidemiology · 2001–2019
A researcher in the Science corpus: 10 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Epidemiology — 40 citations into it
- Cognitive Neuroscience — 13 citations into it
Whom S. Lesage trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts S. Lesage overall
- K. Takeda
- Kate Schroder
- E. K. Kim
- Jonas W. Mueller
- Nibaldo C. Inestrosa
- M. H. Yan
- J. Tschopp
- Shizuo Akira
Papers from S. Lesage's perspective
Ordered by how strongly the researchers S. Lesage trusts endorse each paper. Same corpus, a different order for every researcher.
- Epidemiology of restless legs symptoms in adults. (Archives of Internal Medicine)
- alpha-Synuclein locus triplication causes Parkinson's disease. (Science)
- Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study (Lancet Neurology)
- Prevalence of restless legs syndrome and periodic limb movement disorder in the general population. (Journal of Psychosomatic Research)
- Idiopathic Parkinson's disease: possible routes by which vulnerable neuronal types may be subject to neuroinvasion by an unknown pathogen (Journal of neural transmission)
- Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations. (The Lancet)
- The Sequence Alignment/Map format and SAMtools (Bioinform.)
- Pathological α-Synuclein Transmission Initiates Parkinson-like Neurodegeneration in Nontransgenic Mice (Science)
- Non-motor Symptoms of Parkinson's Disease
- Staging of brain pathology related to sporadic Parkinson's disease. (Neurobiology of Aging)
Their papers
- CARD15 mutations in Blau syndrome (2001) — 984 citations
- Identification of novel risk loci, causal insights, and heritable risk for Parkinson’s disease: a meta-genome wide association study (2019) — 1,651 citations
- G51D α‐synuclein mutation causes a novel Parkinsonian–pyramidal syndrome (2013) — 687 citations
- What genetics tells us about the causes and mechanisms of Parkinson's disease. (2011) — 614 citations
- Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies (2011) — 935 citations
- Multi-center analysis of glucocerebrosidase mutations in Parkinson disease (2009) — 1,060 citations
- Parkinson's disease: from monogenic forms to genetic susceptibility factors. (2009) — 995 citations
- Restless legs syndrome (2003) — 1,172 citations
- CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease. (2002) — 1,033 citations
- Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease (2001) — 5,724 citations